Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F212/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
  • C08F212/02—Monomers containing only one unsaturated aliphatic radical
  • C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
  • C08F212/14—Monomers containing only one unsaturated aliphatic radical containing one ring substituted by heteroatoms or groups containing heteroatoms
  • C08F212/30—Sulfur
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F226/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen
  • C08F226/06—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a heterocyclic ring containing nitrogen
• • G—PHYSICS
  • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
  • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
  • G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
  • G03C8/42—Structural details
  • G03C8/52—Bases or auxiliary layers; Substances therefor
  • G03C8/56—Mordant layers
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
  • Y10S430/142—Dye mordant

Definitions

• This invention relates to a polymer which is an effective mordant for dyes used in photographic elements and a photographic element containing said polymer. More particularly, this invention relates to a mordant for fixing an imagewise-formed diffusible dye and a color photographic element comprising a layer containing said mordant.
• quaternary ammonium salt polymers such as those described in, for example, U.S. Patents 3,709,690, 3,958,995 and 3,898,088, as mordants for fixing anionic dyes. While polymers of this type function as good mordants for anionic dyes, they are deficient in keeping the mordant-fixed dyes in a stable condition.
• a photographic system containing a dye image mordanted with such a dye mordant has another disadvantage in that the mordanted image dye is liable to undergo chemical change or degradation upon exposure to fluorescent light, solar radiation or the like.
• the polymers having a tertiary imidazole ring system in the side chain as described in, for example, British Patent 2,056,101, U.S. Patents 4,115,124, 4,282,305, and 4,273,853, are capable of keeping the mordanted dyes stable against light but are deficient in mordanting activity.
• a polymer which comprises a recurring unit of general formula ( I ) and at least one of recurring units of general formulae ( I I), (III) and (IV) and a photographic element which contains the above-mentioned polymer.
• R 1 , R 2 and R 3 each represents a hydrogen atom or an alkyl group containing 1 to 6 carbon atoms; L is a divalent linking group containing 1 to 20 carbon atoms; and m is 0 or 1.
• R la re p resents a hydrogen atom or an alkyl group containing 1 to 6 carbon atoms.
• R 4 is an alkyl group, an aryl group or an aralkyl group.
• R 5 and R 6 each represents a hydrogen atom or an alkyl group, an alkoxy group, an aryl group or an aralkyl group.
• D is a divalent linking group which is necessary for the formation of a 5- to 7- membered ring with the nitrogen atom and carbonyl group; and n, p and q each is 0 or 1 .
• the polymer according to this invention may contain two or more kinds of monomer units of different general formulae among general formulae (II), (III) and (IV) or two or more kinds of monomer units of one and the same general formula selected from among said general formulae (II), (III) and (IV).
• R 1 , R 2 and R 3 each represents a hydrogen atom or a lower alkyl group of 1 to 6 carbon atoms such as methyl group, ethyl group, n-propyl group, n-butyl group, n-amyl group and n-hexyl group. Preferred are hydrogen atom methyl group and ethyl group.
• L is a divalent linking group containing 1 to about 20 carbon atoms, such as alkylene groups (e.g., methylene group, ethylene group, trimethylene group, hexamethylene group, etc.), phenylene groups (e.g., o-phenylene group, p-phenylene group, m-phenylene group, etc.), arylenealkylene groups (e.g., etc., wherein R - is an alkylene group of 1 to 12 carbon atoms), -CO 2 -, -CO 2 -R 8 - (wherein R 8 is an alkylene group, a phenylene group or an arylenealkylene group), -CONH-R 8 (wherein R 8 is as defined above), (wherein R 1 and R 8 are as defined above), etc.
• alkylene groups e.g., methylene group, ethylene group, trimethylene group, hexamethylene group, etc.
• phenylene groups e.g.,
• Preferred examples of the monomer unit of general formula (I) are as follows.
• R 1a represents a hydrogen atom or a lower alkyl group of 1 to 6 carbon atoms such as methyl group, ethyl group, n-propyl group, n-butyl group, n-amyl group and n-hexyl group. Preferred are hydrogen atom, methyl group and ethyl group.
• R 4 , R 5 and R 6 each is, for example, an alkyl group (e.g., unsubstituted alkyl group such as methyl group, ethyl group, n-propyl group, n-butyl group, isobutyl group, n-amyl group, hexyl group, n-nonyl group, n-decyl group or n-dodecyl group), a substituted alkyl group (e.g., methoxyethyl group, 3-cyanopropyl group, ethoxycarbonylethyl group, acetoxyethyl group, hydroxyethyl group or 2-butenyl group), an aryl group (e.g., phenyl group, tolyl group or naphthyl group), or an aralkyl group (e.g., unsubstituted aralkyl group such as benzyl group, phenetyl group
• Examples of the monomer unit represented by general formula (III) which are usable in the practice of this invention include the monomer units corresponding to the polymers of N-vinyl compounds described in Murahashi, Imoto and Tani: Gosei Kobunshi (Synthetic High Polymers) III, Asakura Shoten (1971), pages 1-51. Preferred examples of the monomer unit represented by general formula (III) are given below. and
• R la represents a hydrogen atom or a lower alkyl group of 1 to 6 carbon atoms such as methyl group, ethyl group, n-propyl group, n-butyl group, n-amyl group and n-hexyl group. Preferred are hydrogen atom, methyl group and ethyl group.
• D represents a divalent linking group which forms, together with the nitrogen atom and carbonyl group, a 5- to 7-membered ring.
• the monomer unit represented by general formula (IV) there may be mentioned the units corresponding to the polymers of N-vinyl compounds described in the above-described Gosei Kobunshi III.
• the linking group D includes divalent groups composed of carbon atoms (e.g., -CH 2 CH 2 CH 2 -, -CH 2 CH 2 CH 2 CH 2 -, -CH 2 CH 2 CH 2 CH 2 -, divalent groups composed of carbon atoms and a nitrogen atom (e.g., , divalent groups composed of carbon atoms and an oxygen atom (e.g., -OCH 2 CH 2 , and divalent groups composed of carbon atoms and a sulfur atom (e.g., -SCH 2 CH 2 -, .
• divalent groups composed of carbon atoms or of carbon atoms and a nitrogen atom are particularly preferred.
• the monomer unit represented by general formula (I) is from 10 to 98 mol%, preferably 40 to 90 mol%,of the total monomer, and the monomer unit represented by general formula (II), (III) or (IV) is from 2 to 60 mol%, preferably 10 to 50 mol%, of the total monomer. Though other monomers may also be contained, their proportion is preferably not more than 40 mol% of the total monomer.
• the molecular weight of the polymer according to this invention is preferably in the range of 5x10 3 to 1x10 7 . If the molecular weight is too low, the polymer tends to migrate, while the use of a polymer of excessively large molecular weight results in coating troubles.
• the most desirable range is 1x10 4 to 2 x 10 6 .
• Preferred examples of the polymer according to this invention are as follows.
• Synthesis examples of the polymer according to this invention are as follows.
• a three-necked flask of 200 ml capacity was charged with 62.0 g of 1-vinylimidazole, 28.4 g of vinyl acetate and 60 ml of ethanol, and after substituting air with nitrogen gas in the flask, the flask was heated to 75°C.
• 1,242 g of 2,2'-azobis(2,4-dimethylvaleronitrile) was added and under constant heating, the reaction was continued for 2 hours, at the end of which time 1.242 g of 2,2'-azobis(2,4-dimethylvaleronitrile) was further added.
• The. heating was further continued for 3 hours, after which the reaction mixture was cooled to room temperature and dialyzed in a cellulose tube by tap water for 2 days, followed by freeze-drying to give 59.5 g of polymer. Yield 66%.
• a three-necked flask of 200 ml capacity was charged with 31.3 g of 1-vinylimidazole, 18.9 g of N-vinyl-2-pyrrolidone and 50.0 g of dimethylformamide, and after substituting air with nitrogen gas in the flask, the flask was heated to 70°C.
• the temperature became constant, 0 . 615 g of 2,2'-azobis(2,4-dimethylvaleronitrile) was added and as the heating was continued, 0.615 g of 2,2'-azobis-(2,4-dimethylvaleronitrile) was further added after 2 and 4 hours, respectively.
• the heating was further continued for 3 hours, after which the reaction mixture was cooled to room temperature, poured in 1.5 l of acetone, and dried in vacuum to give 50.0 g of polymer.
• a three-necked flask of 500 ml capacity was charged with 47.1 g of 1-vinylimidazole, 27.8 g of N-vinyl-2-pyrrolidone, 51.5 g of potassium styrenesulfinate and 200 g of distilled water, and after substituting air with nitrogen gas in the flask, the flask was heated to 75°C.
• the temperature became constant, 0.904 g of 2,2'-azobis(2-amidinopropane)hydrochloride was added and as the heating was continued, 0.904 g of 2,2'-azobis(2-amidinopropane)hydrochloride was further added after 2 and 4 hours, respectively. Then, the heating was further continued for 3 hours, after which the reaction mixture was cooled to room temperature to give 326 g of polymer aqueous solution.
• the polymer according to this invention is used either alone or in combination with a binder in the mordant layer of the photographic element.
• a suitable hydrophilic binder can be used as said binder.
• hydrophilic binder include transparent or translucent hydrophilic colloids such as proteins, e.g., gelatin, gelatin derivatives, etc., cellulose derivatives, polysaccharides, e.g., starch, gum arabic, etc., and other natural substances, as well as synthetic.
• polymers such as polyvinylpyrrolidone, polyacrylamide, polyvinyl alcohol and other water soluble polyvinyl compounds. Preferred are gelatin and polyvinyl alcohol.
• the above-mentioned mordant layer may be present in the light-sensitive material or in the dye fixing material.
• the ratio of the polymer mordant of this invention to the binder and the coating amount of the polymer mordant may be easily selected by those skilled in the art in accordance with the amount of dye to be mordanted, the type and composition of the polymer mordant, the image-forming process used, etc.
• the mordant/binder ratio is 20/80 through 80/20 by weight and the coating amount of the mordant is 0.2 to 15 g/m 2 , preferably 0.5 to 8 g/m 2.
• the mordant layer containing the polymer mordant of this invention may further contain various surfactants for improved coating properties.
• the polymer of this invention may be used in combination with a gelatin hardening agent.
• hardening agent examples include aldehydes (e.g., formaldehyde, glyoxal, glutaraldehyde, etc.), N-methylol compounds (di- methylolurea, methyloldimethylhydantoin, etc.), dioxane derivatives (e.g., 2,3-dihydroxydioxane, etc.), active vinyl compounds [ 1,3,5-triacryloyl hexahydro-s-triazine, bis-(vinylsulfonyl)methylether, N,N'-ethylene bis(vinylsulfonyl- acetamide), N,N'-trimethylene-bis(vinylsulfonylacetamide), etc.], active halogen compounds (2,4-dichloro-6-hydroxy-s-triazine, etc.), mucohalic acids (mucochloric acid, muco- phenoxychloric acid, etc.
• aldehydes aldehydes, active vinyl compounds and active halogen compounds are particularly preferred.
• hardening agents may be added either directly to a coating solution for the mordant layer or, alternatively, to a different coating solution so that it will diffuse into the mordant layer during the multicoating process.
• the amount of said hardening agent for the purposes of this invention can be optionally selected in accordance with the purposes. However, its amount is generally 0.1 to 20 wt% and preferably 1 to 8 wt% based on the weight of gelatin.
• the dye transfer density may be increased by incorporating a metal ion in the dye fixing material.
• a metal ion is incorporated in the mordant layer containing the polymer mordant of this invention or in the layer either over or beneath the mordant layer.
• the metal ion mentioned just above is preferably colorless and stable against heat and light.
• multivalent transition metal ions such as Cu 2+ , Zn 2+ , Ni 2+ , Pt 2+ , P d , CO 3+ , etc. are preferred and Zn 2+ is especially preferred.
• the metal ion is generally added in the form of a water-soluble compound such as ZnS04, Zn(CH 3 CO 2 ) 2 , etc., and its adding amount is 0.01 to 5 g/ m 2 , and preferably 0.1 to 1.5 g/ m 2 .
• hydrophilic binder In the layer to which such a metal ion is added, there may be incorporated a hydrophilic polymer as binder.
• the hydrophilic binder is most commonly a transparent or translucent colloid such as proteins, e.g., gelatin and its derivatives, cellulose derivatives, polysaccharides, e.g., starch, gum arabic, etc., and other natural material as well as synthetic polymers such as polyvinylpyrrolidone, polyacrylamide, polyvinyl alcohol, and other water soluble polyvinyl compounds.
• gelatin and polyvinyl alcohol can be used effectively.
• the image-forming dye which is mordanted on the mordant layer according to this invention includes azo dyes, azomethine dyes, anthraquinone dyes, naphthoquinone dyes, styryl dyes, nitro dyes, quinoline dyes, carbonyl dyes and phthalocyanine dyes, which have anionic groups such as phenolic hydroxy group, sulfonamido group, sulfonyl group, carboxyl group and other groups.
• the mordant layer of this invention can be advantageously employed for fixing the dye in the color image forming process in which a diffusible dye is formed in an imagewise pattern, caused to diffuse and, then, fixed.
• the above-mentioned color image forming process may take various forms such as the process employing a developer at or near room temperature (for example, the process described in Belgian Patent 757,959), the process using heat development (e.g., Japanese Patent Application (OPI) Nos. 58543/83 and 79247/83) (the term "OPI” as used herein means a "publised unexamined Japanese patent application") ,etc., the mordant layer of this invention can be used in any of such image forming processes.
• OPI Japanese Patent Application
• the mordant layer of this invention can be used in any of such image forming processes.
• the dye-providing substance useful for the above-mentioned heat development process may be represented by the general formula (I).
• D represents a dye moiety or a precursor thereof
• Y represents a substrate having such a function as to change the diffusibility of the dye providing substance (I) upon the redox reaction caused in the heat development step.
• change in diffusibility is intended to include the cases wherein (1) the compound (I) is nondiffusible originally, and it is changed into diffusible one or releases a diffusible dye, and (2) the compound (I) is originally diffusible, and changed into nondiffusible one. This change is caused by oxidation of Y or reduction of Y according to the nature of Y, and this two reactions are used appropriately according to the circumstances.
• Y whose diffusibility is changed by oxidation
• dye releasing redox substrates such as p-sulfonamidonaphthols (including p-sulfonamidophenols, and specific examples thereof are described in Japanese Patent Application (OPI) Nos. 33826/73 and 50736/78, and European Patent 76,492), o-sulfonamidophenols (including o-sulfonamidonaphthols, and specific examples thereof are described in Japanese Patent Application (OPI) Nos. 113624/76, 12642/81, 16130/81, 16131/ 81, 4043/82 and 650/82, U.S.
• Patent 4,053,312, and European Patent 76,492 hydroxysulfonamidoheterocyclic rings (with specific examples described in Japanese Patent Application ( O PI) No. 104343/76 and European Patent 76,492), 3-sulfona- midoindoles (with specific examples described in Japanese Patent Application (OPI) Nos. 104343/76, 46730/78, 130122/79 and 85055/82 and European Patent 76,492), a-sulfonamido- ketones (with specific examples described in Japanese Patent Application (OPI) Nos. 3819/78 and 48534/79 and European Patent 76,492, etc.).
• Y of a different type which release a dye by intramolecular nucleophilic attack after oxidation mention may be made of intramolecular assist type substrates described in Japanese Patent Application (OPI) No. 20735/82 and European Patent Application 0106211A.
• Y of another different type which releases a dye by an intramolecular ring closure reaction under alkaline conditions, but causes substantially no release of a dye when oxidized
• substrates which are modifications of the above-described type of Y, and release dyes through winding change caused in an isoxazoline ring by a nucleophilic agent are also useful.
• Y of still another different type mention may be made of substrates which can release their dye moieties through dissociation of acidic proton under alkaline conditions, but cause substantially no release of dyes when oxidized (specific examples of which are described in Japanese Patent Application (OPI) Nos. 69033/78 and 130927/79) .
• examples of Y whose diffusibility is changed by reduction include nitro compounds described in Japanese Patent Application (OPI) No. 110827/78 and quinone compounds described in Japanese Patent Application (OPI) No. 110827/78 and U.S. Patents 4,356,249 and 4,358,525. These compounds are reduced by a reducer (called an electron donor) remaining without consumed in the heat development process to produce nucleophilic groups, and release dyes through the molecular attack of the resulting nucleophilic groups.
• a reducer called an electron donor
• Substrate of the quinone type which are modification of the above-described quinone compounds, and release their dye moieties through dissociation of acidic proton of the reductant thereof are also useful.
• materials capable of releasing mobile dyes through the reaction with silver ion present in a light-sensitive material can be employed, and are described in Japanese Patent Application (OPI) No. 180548/84.
• Such a photographic element using the mordant dye according to this invention generally consists of 1) a support, 2) a light-sensitive element and 3) an image-receiving element, and the development may be effected by heating or with a developing agent.
• the photographic element is first imagewise exposed and, then, the silver halide is developed, whereupon a diffusible dye is fprmed in the corresponding imagewise pattern and migrates onto the image-receiving element.
• the light-sensitive element and image-receiving element mentioned above may be disposed either on one and the same support or on independent supports.
• a developing agent an auxiliary developing agent and other processing agents may further be incorporated.
• the pH of the resulting benzotriazole silver emulsion is adjusted to cause precipitation and the excess salt is removed.
• the pH is then adjusted to 6.0, whereby 400 g of a benzotriazole silver emulsion is obtained.
• a cyan dye providing substance of the structure shown below 0.5 c of sodium 2-ethylhexyl succinate sulfonate and 5 9 cf tricresyl phosphate (TCP) are weighed and dissolved in 30 ml of ethyl acetate under heating at about 60°C to give a homogeneous solution.
• This solution is mixed with 100 g of a 10% solution of lime-treated gelatin with stirring and dispersed by means of a homogenizer at 10,000 r.p.m. for 10 minutes.
• the dispersion is referred to as "a dispersion of the dye providing substance (cyan)".
• the following ingredients are mixed and dissolved and the mixture is coated on a polyethylene terephthalate film in a wet thickness of 30 ⁇ m, followed by drying.
• gelatin hardening agent H-1 and 0.25 g of gelatin hardening agent H-2 are added to 160 ml of distilled water, followed by addition of 100 g of 10% acid- treated gelatin, and the mixture is evenly stirred.
• a paper support laminated with a polyethylene film containing titanium oxide as dispersed therein is uniformly coated with the above mixture in a wet thickness of 60 ⁇ m, followed by drying.
• 10 g of mordant HP-1 and 200 ml of distilled water are added, followed by addition of 100 g of 10% lime-treated gelatin.
• the mixture is evenly stirred and coated on the above layer in a wet thickness of 85 um, followed by drying. This is referred to as "dye fixing material (A) containing mordant HP-1".
• Dye fixing materials (B), (C) and (D) are prepared in the same manner as above except that 14.6 g of P-3, 16.1 g of P-8 and 26.8 g of P-11 are respectively used in lieu of the above mordant HP-1.
• the above light-sensitive material was imagewise exposed to light at 2000 lux using a tungsten lamp and heated uniformly on a heat block at 130°C for 30 seconds. Then, 10 ml/m 2 of water was applied on the coated side of the dye fixing material., which was then brought into contact with the coated side of the above heat-treated light-sensitive material and the assembly was heated on a heat block at 80°C for 5 seconds, after which the dye fixing material was separated from the light-sensitive material, whereupon a cyan color negative image was obtained on the dye fixing material.
• the density of the negative image was measured by means of a Macbeth reflection densitometer RD-519.
• Example 2 The procedure of Example 2 was performed in the same manner as in Example 1 except that the dye providing substance having the following structure was used in lieu of the cyan dye providing substance in the light-sensitive material of Example 1. The results are shown in Table 2.
• Example 3 The procedure of Example 3 was performed in the same manner as in Example 1 except that the dye providing substance having the following structure was used in lieu of the cyan dye providing substance in the light-sensitive material of Example 1. The results are shown in Table 3.
• mordant according to this invention provides a yellow color image with an extremely high transfer density.
• a dye fixing layer (E) (using HP-1) was prepared by coating the following layers on a polyethylene terephthalate support containing dispersed titanium oxide.
• the ingredients (a) through (f) were mixed and dissolved and the solution was uniformly coated on a layer as wet thickness of 90 ⁇ m.
• the light-sensitive material was imagewise exposed at 2000 lux using a tungsten lamp for 1C seconds and, then, heated uniformly on a heat block at 140°C for 20 seconds.
• the coated side of thus heat-treated light-sensitive material was brought into contact with the coated side of the above dye fixing material and the assembly was passed through a heated roller at 130°C for 40 seconds, whereby it was heated under pressure. Then, the dye fixing material was separated from the light-sensitive material, whereupon a cyan positive color image to the silver image was obtained on the color fixing material. The density of this negative image to red light was measured by means of a M acbeth reflection densitometer RD 519.
• the mordant according to this invention provides a cyan color image having an extremely high transfer density.
• Example 5 The procedure of Example 5 was performed in the same manner as in Example 4 except that the magenta dye providing substance of Example 2 was used in lieu of the cyan dye providing substance in the light-sensitive material of Example 4. The results are shown in Table 5.
• the mordant according to this invention does not reduce but rather improves the fastness of the transferred color image and provides a magenta color image having a high density.
• Example 6 The procedure of Example 6 was performed in the same manner as in Example 4 except that the yellow dye providing substance of Example 3 was used in lieu of the cyan dye providing substance in the light-sensitive material of Example 4. The results are shown in Table 6.
• the mordant according to this invention exhibits an excellent characteristic for all of cyan, magenta and yellow dyes by providing transferred images of extremely high density without loss in the light fastness of the dye images.

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• Polymers & Plastics (AREA)
• Medicinal Chemistry (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Health & Medical Sciences (AREA)
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• General Physics & Mathematics (AREA)
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• Engineering & Computer Science (AREA)
• Physics & Mathematics (AREA)
• Thermal Transfer Or Thermal Recording In General (AREA)
• Silver Salt Photography Or Processing Solution Therefor (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
• Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)

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• 1984
  • 1984-05-08 JP JP59091620A patent/JPS60235134A/ja active Granted
• 1985
  • 1985-05-03 EP EP85105416A patent/EP0160947B1/de not_active Expired - Lifetime
  • 1985-05-03 DE DE8585105416T patent/DE3579031D1/de not_active Expired - Lifetime
• 1987
  • 1987-08-17 US US07/086,245 patent/US4766052A/en not_active Expired - Lifetime

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